ClinVar Miner

Submissions for variant NM_000249.4(MLH1):c.306+2dup

dbSNP: rs267607738
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
International Society for Gastrointestinal Hereditary Tumours (InSiGHT) RCV000075629 SCV000106631 pathogenic Lynch syndrome 1 2018-06-13 reviewed by expert panel curation Variant at IVS±2

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